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- NP668461.RALqrepnFKjFhls9j6BasL7Gv08Stjts5_KyQ5-0a1Aw8130_assertion type Assertion NP668461.RALqrepnFKjFhls9j6BasL7Gv08Stjts5_KyQ5-0a1Aw8130_head.
- NP668461.RALqrepnFKjFhls9j6BasL7Gv08Stjts5_KyQ5-0a1Aw8130_assertion description "[Autosomal recessive ichthyosis with hypotrichosis (ARIH) syndrome, which is characterized by congenital ichthyosis, abnormal hair and corneal involvement, has recently been shown in one consanguineous Israeli Arab family to be caused by a mutation in the ST14 gene, which encodes serine protease matriptase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668461.RALqrepnFKjFhls9j6BasL7Gv08Stjts5_KyQ5-0a1Aw8130_provenance.
- NP668461.RALqrepnFKjFhls9j6BasL7Gv08Stjts5_KyQ5-0a1Aw8130_assertion evidence source_evidence_literature NP668461.RALqrepnFKjFhls9j6BasL7Gv08Stjts5_KyQ5-0a1Aw8130_provenance.
- NP668461.RALqrepnFKjFhls9j6BasL7Gv08Stjts5_KyQ5-0a1Aw8130_assertion SIO_000772 18445049 NP668461.RALqrepnFKjFhls9j6BasL7Gv08Stjts5_KyQ5-0a1Aw8130_provenance.
- NP668461.RALqrepnFKjFhls9j6BasL7Gv08Stjts5_KyQ5-0a1Aw8130_assertion wasDerivedFrom befree-2016 NP668461.RALqrepnFKjFhls9j6BasL7Gv08Stjts5_KyQ5-0a1Aw8130_provenance.
- NP668461.RALqrepnFKjFhls9j6BasL7Gv08Stjts5_KyQ5-0a1Aw8130_assertion wasGeneratedBy ECO_0000203 NP668461.RALqrepnFKjFhls9j6BasL7Gv08Stjts5_KyQ5-0a1Aw8130_provenance.